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我如何诊断和治疗原发性骨髓纤维化纤维化前期(pre-PMF)患者——2024年德国专家小组讨论的实用方法

How I diagnose and treat patients in the pre-fibrotic phase of primary myelofibrosis (pre-PMF) - practical approaches of a German expert panel discussion in 2024.

作者信息

Griesshammer Martin, Al-Ali Haifa Kathrin, Eckardt Jan-Niklas, Fiegl Michael, Göthert Joachim, Jentsch-Ullrich Kathleen, Koschmieder Steffen, Kvasnicka Hans Michael, Reiter Andreas, Schmidt Burkhard, Heidel Florian H

机构信息

Oncology, Haemostaseology and Palliative Care, Johannes Wesling Medical Center Minden, University Clinic for Hematology, University of Bochum, Bochum, Germany.

Krukenberg Cancer Center, University Hospital of Halle, Halle, Germany.

出版信息

Ann Hematol. 2025 Jan;104(1):295-306. doi: 10.1007/s00277-025-06191-7. Epub 2025 Jan 31.

Abstract

The prefibrotic phase of primary myelofibrosis (pre-PMF) represents a distinct subentity within the spectrum of myeloproliferative neoplasms (MPNs), recognized by the World Health Organization (WHO) and the International Consensus Classification (ICC). Pre-PMF is characterized by unique morphological, clinical, and molecular features, distinguishing it from essential thrombocythemia (ET) and overt myelofibrosis (overt-PMF). The diagnostic process for pre-PMF relies on bone marrow histology, identification of molecular mutations and exclusion of other myeloid neoplasms. Misclassification remains a significant challenge due to overlapping phenotypes and the heterogeneity of clinical presentations, which range from asymptomatic cases to severe cytopenias and a high thrombotic risk. Management strategies for pre-PMF focus on mitigating symptom burden, reducing thromboembolic events, and preventing disease progression. Low-risk patients often benefit from observational approaches or low-dose aspirin, while cytoreductive therapies, such as hydroxyurea or interferon-alpha, are utilized in symptomatic or high-risk cases. JAK inhibitors like ruxolitinib have shown promise in addressing splenomegaly and systemic symptoms, although their role in pre-PMF requires further investigation. Advances in artificial intelligence are enhancing diagnostic precision by refining bone marrow histopathological analysis, paving the way for more accurate disease classification and tailored therapeutic strategies. This position paper integrates insights from a German expert panel discussion, underscoring the need for interdisciplinary collaboration, adherence to updated WHO/ICC diagnostic criteria, and personalized treatment approaches. By addressing diagnostic challenges and therapeutic nuances, it seeks to improve outcomes and quality of life for patients navigating the complexities of pre-PMF.

摘要

原发性骨髓纤维化的纤维化前期(pre-PMF)是骨髓增殖性肿瘤(MPN)谱系中的一个独特亚实体,已被世界卫生组织(WHO)和国际共识分类(ICC)所认可。Pre-PMF具有独特的形态学、临床和分子特征,使其有别于原发性血小板增多症(ET)和明显骨髓纤维化(overt-PMF)。Pre-PMF的诊断过程依赖于骨髓组织学检查、分子突变的鉴定以及其他髓系肿瘤的排除。由于表型重叠和临床表现的异质性,误诊仍然是一个重大挑战,临床表现范围从无症状病例到严重血细胞减少和高血栓形成风险。Pre-PMF的管理策略侧重于减轻症状负担、减少血栓栓塞事件以及预防疾病进展。低风险患者通常受益于观察性方法或低剂量阿司匹林,而对于有症状或高风险病例,则采用细胞减灭疗法,如羟基脲或α干扰素。像鲁索替尼这样的JAK抑制剂在解决脾肿大和全身症状方面已显示出前景,尽管它们在pre-PMF中的作用还需要进一步研究。人工智能的进展通过完善骨髓组织病理学分析提高了诊断精度,为更准确的疾病分类和个性化治疗策略铺平了道路。本立场文件整合了德国专家小组讨论的见解,强调了跨学科合作、遵循最新的WHO/ICC诊断标准以及个性化治疗方法的必要性。通过应对诊断挑战和治疗细微差别,它旨在改善应对pre-PMF复杂性的患者的治疗结果和生活质量。

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